Search research articles
Contact Us
Filters
Showing results (1-10 of 14) with videos related to
Page
of 2
Sort By:
American Journal of Medical Genetics
|
April 15, 2000
Spondylocarpotarsal synostosis syndrome and cervical instability
L H Seaver, E Boyd
Pediatric Clinics of North America
|
February 1, 1992
Teratology in pediatric practice
L H Seaver, H E Hoyme
American Journal of Medical Genetics
|
December 15, 1991
New syndrome: mother and son with hypertelorism, downslanting palpebral fissures, malar hypoplasia, and apparently low-set ears associated with joint and scrotal anomalies
L H Seaver, S B Cassidy
American Journal of Medical Genetics
|
May 15, 1994
Female pseudohermaphroditism with multiple caudal anomalies: absence of Y-specific DNA sequences as pathogenetic factors
L H Seaver, J Grimes, R P Erickson
Clinical Genetics
|
March 1, 1995
A family with unusual Waardenburg syndrome type I (WSI), cleft lip (palate), and Hirschsprung disease is not linked to PAX 3
J W Pierpont, D St Jacques, L H Seaver, et al.
Pediatrics
|
February 1, 1994
Toluene embryopathy: delineation of the phenotype and comparison with fetal alcohol syndrome
M A Pearson, H E Hoyme, L H Seaver, et al.
JIMD Reports
|
October 3, 2013
Clinical Presentation and Positive Outcome of Two Siblings with Holocarboxylase Synthetase Deficiency Caused by a Homozygous L216R Mutation
T P Slavin, S J Zaidi, C Neal, et al.
American Journal of Medical Genetics
|
April 15, 1993
Congenital scalp defects and vitreoretinal degeneration: redefining the Knobloch syndrome
L H Seaver, L Joffe, R P Spark, et al.
American Journal of Medical Genetics
|
October 22, 1998
Isolated hemihyperplasia (hemihypertrophy): report of a prospective multicenter study of the incidence of neoplasia and review
H E Hoyme, L H Seaver, K L Jones, et al.
Journal of Medical Genetics
|
November 1, 1994
Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndrome
L H Seaver, J W Pierpont, R P Erickson, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
American Journal of Medical Genetics
|
April 15, 2000
Spondylocarpotarsal synostosis syndrome and cervical instability
L H Seaver, E Boyd
Pediatric Clinics of North America
|
February 1, 1992
Teratology in pediatric practice
L H Seaver, H E Hoyme
American Journal of Medical Genetics
|
December 15, 1991
New syndrome: mother and son with hypertelorism, downslanting palpebral fissures, malar hypoplasia, and apparently low-set ears associated with joint and scrotal anomalies
L H Seaver, S B Cassidy
American Journal of Medical Genetics
|
May 15, 1994
Female pseudohermaphroditism with multiple caudal anomalies: absence of Y-specific DNA sequences as pathogenetic factors
L H Seaver, J Grimes, R P Erickson
Clinical Genetics
|
March 1, 1995
A family with unusual Waardenburg syndrome type I (WSI), cleft lip (palate), and Hirschsprung disease is not linked to PAX 3
J W Pierpont, D St Jacques, L H Seaver, et al.
Pediatrics
|
February 1, 1994
Toluene embryopathy: delineation of the phenotype and comparison with fetal alcohol syndrome
M A Pearson, H E Hoyme, L H Seaver, et al.
JIMD Reports
|
October 3, 2013
Clinical Presentation and Positive Outcome of Two Siblings with Holocarboxylase Synthetase Deficiency Caused by a Homozygous L216R Mutation
T P Slavin, S J Zaidi, C Neal, et al.
American Journal of Medical Genetics
|
April 15, 1993
Congenital scalp defects and vitreoretinal degeneration: redefining the Knobloch syndrome
L H Seaver, L Joffe, R P Spark, et al.
American Journal of Medical Genetics
|
October 22, 1998
Isolated hemihyperplasia (hemihypertrophy): report of a prospective multicenter study of the incidence of neoplasia and review
H E Hoyme, L H Seaver, K L Jones, et al.
Journal of Medical Genetics
|
November 1, 1994
Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndrome
L H Seaver, J W Pierpont, R P Erickson, et al.
Page
of 2